Danish Isravel Antony, Prasad Karnam Jayarampillai Rajendra
Department of Chemistry, Bharathiar University, Coimbatore-641046, India.
Acta Pharm. 2003 Dec;53(4):287-94.
1-Oxo-1,2,3,4-tetrahydrocarbazoles (1a-e) upon mixed aldol condensation with o-nitrobenzaldehyde (2) yielded 13-oxo-quino[3,4-b]carbazol-N-oxides (3a-e). All the prepared compounds were characterized by elemental and spectral analysis. A plausible mechanism for the formation of the final products is proposed. The title compounds proved to have great potentialities as antibacterial and antifungal agents due to the presence of the N-oxide group. Particularly, the chloro substituted derivative, 3d, showed excellent antimicrobial activity.
1-氧代-1,2,3,4-四氢咔唑(1a - e)与邻硝基苯甲醛(2)进行混合羟醛缩合反应,生成了13-氧代喹啉并[3,4 - b]咔唑 - N - 氧化物(3a - e)。所有制备的化合物均通过元素分析和光谱分析进行了表征。提出了形成最终产物的合理机制。由于存在N - 氧化物基团,标题化合物被证明具有作为抗菌和抗真菌剂的巨大潜力。特别是,氯取代衍生物3d表现出优异的抗菌活性。